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体内金-咪唑自组装复合物的检测:近红外表面增强拉曼散射信号报告分子。

In vivo detection of gold-imidazole self-assembly complexes: NIR-SERS signal reporters.

作者信息

Souza Glauco R, Levin Carly S, Hajitou Amin, Pasqualini Renata, Arap Wadih, Miller J Houston

机构信息

Department of Chemistry, The George Washington University, Washington, D.C. 20052, USA.

出版信息

Anal Chem. 2006 Sep 1;78(17):6232-7. doi: 10.1021/ac060483a.

Abstract

Here we report in vitro and in vivo detection of self-assembled Au-imidazole by using near-infrared surface-enhanced Raman scattering (NIR-SERS). In vivo, the Au-imidazole structures were administered into tumor-bearing mice and detected noninvasively. The self-assembled Au-imidazole complexes were generated by the adsorption of imidazole molecules onto Au nanoparticles (NP) and were then characterized as aqueous suspensions by using NIR-SERS, angle-dependent light scattering with fractal dimension analysis, and visible extinction spectroscopy. The structure and optical activity was sensitive to imidazole concentration and Au NP size. Specifically, the Au-imidazole assemblies formed at lower imidazole concentrations had the lowest fractal dimension (D(f) = 1.2) and the largest Raman enhancement factors for the dominant NIR-SERS feature, a ring-breathing vibrational mode at 954 cm(-1). Changes in elastic scattering intensity, fractal dimension, and surface plasmon absorption were observed with increasing imidazole concentration. The Raman enhancement factor was also found to range between 10(6) and 10(9) with different primary Au nanoparticle sizes. For the higher enhancement factor systems, NIR-SERS detection of Au-imidazole was performed with data acquisitions time of only 5 s. The largest enhancement was observed for the 954-cm(-1) feature at an imidazole concentration of 1.9 microM when coupled to 54-nm-diameter Au NPs (the largest NP tested). Finally, we show the first demonstration of in vivo, noninvasive, and real-time SERS detection.

摘要

在此,我们报告了利用近红外表面增强拉曼散射(NIR-SERS)对自组装金-咪唑进行的体外和体内检测。在体内,将金-咪唑结构施用于荷瘤小鼠并进行无创检测。自组装金-咪唑复合物是通过咪唑分子吸附到金纳米颗粒(NP)上生成的,然后利用NIR-SERS、具有分形维数分析的角度相关光散射和可见消光光谱对其作为水悬浮液进行表征。其结构和光学活性对咪唑浓度和金纳米颗粒大小敏感。具体而言,在较低咪唑浓度下形成的金-咪唑组装体具有最低的分形维数(D(f)=1.2)以及对于主要NIR-SERS特征(954 cm(-1)处的环呼吸振动模式)最大的拉曼增强因子。随着咪唑浓度增加,观察到弹性散射强度、分形维数和表面等离子体吸收的变化。还发现不同初始金纳米颗粒大小的拉曼增强因子在10(6)到10(9)之间。对于具有较高增强因子的系统,仅用5 s的数据采集时间就进行了金-咪唑的NIR-SERS检测。当与直径54 nm的金纳米颗粒(测试的最大纳米颗粒)偶联时,在咪唑浓度为1.9 microM时观察到954-cm(-1)特征的最大增强。最后,我们展示了首次体内无创实时SERS检测的实例。

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